VIA Microcatheter

VIA 33 Microcatheter

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

Concentrated in Jiangsu (3), Shanghai (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRA
Manufacturer City Province Registered as Device types
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Vascupatent Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 1

Record

Regulatory record for VIA Microcatheter
Listed by Sequent Medical, Inc., United States
FDA product code KRA
Device type Catheter, Continuous Flush
Device class Class 2
Regulation 21 CFR 870.1210
Record published 2016-07-12
Record revised 2021-12-22 (version 10)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Special storage condition: Store at a controlled room temperature in a dry place
Sizes Lumen/inner diameter 0.0175 to 0.033 in

Catalogue Numbers

Catalogue numbers for VIA Microcatheter
Catalogue number Size Status
VIA-33-133-01 Lumen/Inner Diameter 0.033 in In distribution
VIA-27-154-01 Lumen/Inner Diameter 0.027 in In distribution
VIA-21-154-01 Lumen/Inner Diameter 0.021 in In distribution
VIA-17-154-01 Lumen/Inner Diameter 0.0175 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fountain® Merit Medical Systems, Inc. 154
PulseSpray AngioDynamics, Inc. 149
Merit Maestro® Merit Medical Systems, Inc. 143
Phenom™ Catheter Cathera, Inc. 103
UniFuse AngioDynamics, Inc. 84
CXI Cook Incorporated 48
Uni-Fuse+ AngioDynamics, Inc. 32
Prowler Medos International Sàrl 27
Truwave, Vamp Edwards Lifesciences Technology Sarl 26
ICU Medical ICU Medical, Inc 21
Cantata Cook Incorporated 20
Truwave, Vamp Plus Edwards Lifesciences Technology Sarl 19

Showing 12 of 149. All products under Catheter, Continuous Flush

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K123477 2013-03-19

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2016-09-23 Class II Under Investigation by firm Sequent Medical is recalling the VIA 27 Microcatheter because it may not adequately re-sheath the interventional device into the catheter as designed. 618 units 2017-05-01

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer